ClinConnect ClinConnect Logo
Search / Trial NCT06380179

Photomedicine Project 14: PBMT for Performance Enhancement in SOF

Launched by MUSCULOSKELETAL INJURY REHABILITATION RESEARCH FOR OPERATIONAL READINESS (MIRROR) · Apr 18, 2024

Trial Information

Current as of July 01, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial, called the Photomedicine Project 14, is studying a treatment known as Photobiomodulation Therapy (PBMT) to see if it can help Special Operations Forces (SOF) improve their physical performance and recovery after intense training. PBMT involves using a low-level laser on the body, which may enhance healing and reduce fatigue. The researchers want to find out how this treatment affects both the physical and mental performance of SOF operators after they exercise.

To be eligible for this study, participants must be active-duty Special Forces personnel who can understand and read English, and who are able to participate in coach-led training without any restrictions. However, individuals who are obese, have certain medical conditions, or take specific medications will not be able to join. Those who participate will receive either the PBMT treatment or a placebo (a treatment that doesn’t contain the active therapy) after their workouts. The study aims to provide valuable insights into whether PBMT can be a useful tool for enhancing performance and recovery in military training.

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • Active-Duty Special Forces Personnel (18-series)
  • Able to read and understand English language for consent purposes
  • Able to commit to study intervention and follow-up
  • Able to participate in THOR3 coach-lead training, without restriction
  • Exclusion Criteria:
  • Obese (body fat \> 25%)
  • Cardiovascular disease
  • Use of select medications (e.g., statins, diuretics, hypertensive agents)
  • Female
  • Tattoo in treatment area (body region)
  • Diagnosis with porphyria (light induced allergy) or photosensitive eczema
  • Current use of medications associated with sensitivity to heat or light (e.g., amiodarone, chlorpromazine, doxycycline, hydrochlorothiazide, nalidixic acid, naproxen, piroxicam, tetracycline, thioridazine, voriconazole)
  • Use of pacemaker/underlying cardiac disease
  • Diagnosed with autoimmune disease(s)
  • Albinism
  • Peripheral Neuropathy

About Musculoskeletal Injury Rehabilitation Research For Operational Readiness (Mirror)

The Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) is a clinical trial sponsor dedicated to advancing the understanding and treatment of musculoskeletal injuries within operational contexts. Focused on enhancing rehabilitation strategies, MIRROR conducts rigorous research to evaluate innovative interventions aimed at optimizing recovery and functional readiness for individuals in high-demand environments. By fostering collaboration among healthcare professionals, researchers, and operational personnel, MIRROR seeks to improve outcomes for those affected by musculoskeletal injuries, ultimately contributing to enhanced performance and resilience in critical operational roles.

Locations

Joint Base Lewis Mcchord, Washington, United States

Patients applied

0 patients applied

Trial Officials

Bradley H Cornell, DPT

Principal Investigator

1st Special Forces Group Tactical Human Optimization, Rapid Rehabilitation and Reconditioning (THOR3)

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported